Van Zele Thibaut, Kitice Adriano, Vellutini Eduardo, Balsalobre Leonardo, Stamm Aldo
Department of Otorhinolaryngology, Ghent University Hospital, Ghent, Belgium.
Allergy Rhinol (Providence). 2013 Summer;4(2):e100-4. doi: 10.2500/ar.2013.4.0053.
Transclival meningoceles and primary spontaneous cerebrospinal fluid (CSF) leaks at the clivus are extremely rare lesions and only few of them have been reported in the literature. We report here six cases of transclival primary spontaneous CSF leaks through the clivus. A retrospective case study was performed. We reviewed six cases involving sinonasal CSF leaks located at the clivus treated between 1997 and 2009. Presenting symptoms, duration of symptoms, defect size, site of defect, surgical approach and technique of defect closure, intraoperative complications, postoperative complications, and recurrences are discussed. All CSF leaks were located in the upper central part of the clivus. two of six patients showed signs of increased intracranial pressure (ICP) including arachnoid pits and/or empty sella. For three patients a purely transnasal approach was used with multilayer reconstruction using a nonvascularized graft, and three patients underwent a transnasal transseptal approach with a multilayer reconstruction, with nasoseptal flap. No recurrences of CSF leaks at clivus or other sites were observed to date with a mean follow-up of 10.3 years (range, 3-15 years). Spontaneous CSF rhinorrhea located at the clivus is an extremely rare condition. To date, only eight cases have been described. Here, we report the largest group of six consecutive cases. Irrespective of the used reconstruction technique in all cases a 100% closure rate was achieved. However, identification of increased ICP is an essential aspect and this condition should be treated either medically or surgically.
经斜坡的脑膜膨出和斜坡原发性自发性脑脊液(CSF)漏是极其罕见的病变,文献中仅有少数病例报道。我们在此报告6例经斜坡的原发性自发性CSF漏病例。进行了一项回顾性病例研究。我们回顾了1997年至2009年间治疗的6例位于斜坡的鼻旁窦CSF漏病例。讨论了临床表现、症状持续时间、缺损大小、缺损部位、手术入路及缺损闭合技术、术中并发症、术后并发症和复发情况。所有CSF漏均位于斜坡的上部中央。6例患者中有2例出现颅内压(ICP)升高的体征,包括蛛网膜颗粒和/或空蝶鞍。3例患者采用单纯经鼻入路,使用非血管化移植物进行多层重建,3例患者采用经鼻经鼻中隔入路,使用鼻中隔瓣进行多层重建。平均随访10.3年(范围3 - 15年),至今未观察到斜坡或其他部位CSF漏复发。位于斜坡的自发性CSF鼻漏是一种极其罕见的疾病。迄今为止,仅描述了8例病例。在此,我们报告最大的一组连续6例病例。无论采用何种重建技术,所有病例均实现了100%的闭合率。然而,识别ICP升高是一个重要方面,这种情况应进行药物或手术治疗。